A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017727



Internal ID19106944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144212130..144378798hg38UCSC Ensembl
Innerchr7:143909223..144075891hg19UCSC Ensembl
Innerchr7:143540156..143706824hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38166669
hg19166669
hg18166669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6735n100
Supporting Variantsnssv3672585, nssv3672586, nssv3756147
Samples
Known GenesARHGEF34P, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017727
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer